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Propanedioic acid, (phenylseleno)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89046-37-7

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89046-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89046-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,4 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89046-37:
(7*8)+(6*9)+(5*0)+(4*4)+(3*6)+(2*3)+(1*7)=157
157 % 10 = 7
So 89046-37-7 is a valid CAS Registry Number.

89046-37-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-phenylselanylpropanedioate

1.2 Other means of identification

Product number -
Other names diethyl 2-phenylselenomalonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89046-37-7 SDS

89046-37-7Relevant academic research and scientific papers

Acridine Orange Hemi(Zinc Chloride) Salt as a Lewis Acid-Photoredox Hybrid Catalyst for the Generation of α-Carbonyl Radicals

Das, Sanju,Mandal, Tanumoy,De Sarkar, Suman

, p. 755 - 765 (2021/12/10)

A readily accessible organic-inorganic hybrid catalyst is reported for the reductive fragmentation of α-halocarbonyl compounds. The robust hybrid catalyst is a self-stabilizing combination of ZnCl2 Lewis acid and acridine orange as the photoactive organic dye. Mechanistic specifics of this hybrid catalyst have been studied in detail using both photophysical and electrochemical experiments. A systematic study enabled the discovery of the appropriate Lewis acid for the effective LUMO stabilization of α-halocarbonyl compounds and thereby lowering of reduction potential within the range of a standard organic dye. This strategy resolves the issues like dehalogenative hydrogenation or homo-coupling of alkyl radicals by guiding the photoredox cycle through an oxidative quenching pathway. The cooperativity between the photoactive organic dye and the Lewis acid counterparts empowers functionalization with a wide range of coupling partners through efficient and controlled generation of alkyl radicals and serves as an appropriate alternative to the expensive late transition metal-based photocatalysts. To demonstrate the application potential of this cooperative catalytic system, four different synthetic transformations of α-carbonyl bromides were explored with broad substrate scopes.

The reaction of phenylselenenyl triflate with diazo compounds

Curini,Epifano,Marcotullio,Rosati

, p. 1813 - 1815 (2007/10/03)

The reaction of phenylselenenyl triflate with diazo compounds is described. Diazoalkanes, α-diazoketones and α-diazoesters gave the corresponding di(phenylselanyl) derivatives either at 0 °C or at room temperature, α-Diazo-β-dicarbonyl compounds gave selectively di(phenylselanyl) derivatives at - 78 °C, while they gave a mixture of di(phenylselanyl)- and mono(phenylselanyl) derivatives either at 0 °C or at room temperature.

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